A shocking report written by Mathilde Debord, first published in Lepointcritique.fr claims that mRNA COVID-19 shots may contribute to cancer development in 17 ways- based on over 100 studies.
Thank you to all the brave doctors & scientists and all the people of the world with curiosity, integrity, and strength of character who have risked so much to get this info out into the world.
The mRNA shots were/are always going to be an immunological catastrophe for humanity.
The mechanism of action (using mRNA instructions to turn one’s own cells into foreign non-self “spike protein factories”) is the primary mechanism of harm.
The primary danger of the COVID-19 mRNA injections has always been one’s own immune system’s attack response by the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells):
The COVID-19 mRNA injections must be recalled from the market and mRNA-based products must be banned because the modified mRNA-LNP genetic technology platform is fundamentally flawed & dangerous by design.
These modified mRNA-LNP COVID-19 injections, that trigger one's own immune system to attack & kill one's own formerly healthy cells (that have been instructed to produce/express foreign, non-self proteins), no matter where those cells are in the body, never should have been made available to the public in the first place.
When the (designed to be long-lasting) n1-methyl pseudouridine modified mRNA transfects one's cells, and gives instructions for the ribosomes to make & express foreign non-self proteins (such as the toxic SARS-CoV-2 spike protein), one's immune system sends the CD8+ cytotoxic T lymphocytes (CTLs) to kill those formerly healthy cells that are now making & expressing non-self proteins.
It is the mission of these CD8+ CTLs to seek out and destroy any such transfected cell that is making foreign non-self proteins. That’s what they do…
Due to the biodistribution properties of the lipid nanoparticles, the encased modified mRNA can go anywhere in the body, including crossing the blood-brain and placental barriers...The LNP "delivery vehicles" traveled to different parts of the body in different people.
Expressing any foreign protein is fatal to the cell doing the expressing. The reason is, our bodies are protected by being able to distinguish ourselves from things that shouldn't be there. Anything non-self will trigger immune destruction of the cells & tissues involved.
Some people will express lots of foreign proteins in vulnerable locations. Others express less in less vulnerable areas.
The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms…
If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signaling (increasing your risk of fast-growing and aggressive cancers)…
And more…
There's no limit to the horrible consequences of injecting into your body something that triggers your own immune system to attack & kill your own formerly healthy cells & tissues.
The public “health” agencies, the COVID “authorities”, & the “mainstream” media fraudulently marketed these experimental mRNA gene “therapy” products as “safe & effective vaccines”. Trusting people thought that they were being presented with the choice (or the mandate) as to whether or not to take a “safe & effective vaccine”…But that was/is a deceptively false “choice”…
The COVID-19 mRNA injections are NOT safe, they are NOT effective, and they are NOT vaccines.
These modified mRNA-LNP gene “therapy” injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the fraudulent mislabeling as “vaccines”. (And because of the EUA & “countermeasure” designations under the Project BioShield Act & PREP Act).
NO ONE should have ever had the “choice” of taking these gene “therapy” injections because the modified mRNA-LNP genetic technology platform is fundamentally flawed & dangerous by design.
The danger is NOT limited to just getting more COVID “boosters”. ANY mRNA gene “therapy” product that transfects your cells and instructs those cells to produce foreign non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues (the role of the Killer T-cells is to monitor ALL the cells of the body, ready to destroy/kill any that express foreign, non-self proteins). This makes EVERY mRNA-based injected product harmful by design.
No one who took these modified mRNA-LNP COVID injections made an informed decision. Most people had no clue about what they allowed to be injected into their bodies...
Also most people still do not understand that the devastating harms inflicted upon people over the last few years was intentional:
AFTER the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells) attack response to modified mRNA transfected cells of tissues & organs inside your body:
After the primary immune system attack response by the cytotoxic T lymphocytes (CTLs), resulting in varying degrees of tissue damage & pathology in different people, a lot happens...
The CTLs will not be able to kill every cell making non-self (spike) protein, so some amount of foreign (spike) protein will get made & released from your cells. That amount will also vary from person to person.
Specialized cells called antigen-presenting cells, especially dendritic cells and macrophages, spring into action. Long story short…you will get serum antibodies made against those foreign proteins which is the stated goal of any shot called a vaccine.
But that can take up to 2 weeks, and during that time, the foreign non-self (spike) proteins are biologically active and will attach to various cellular receptors, resulting in a whole new level of possible tissue destruction.
Now your immune system will activate macrophages & neutrophils that will kill THOSE cells through inflammatory pathways, regardless of whether or not the non-self proteins are toxic themselves.
And if the non-self proteins ARE toxic, like the pathogenic spike proteins, they can cause problems like tissue damage all by themselves without your immune system even being involved at that point.
But your adaptive immune system has done its job & you've made your serum antibodies by now! Yippee!
Too bad those (non-neutralizing, leaky) serum antibodies can only REACT to a (SARS-CoV-2) infection...it is biologically impossible for serum antibodies (in the blood) to PREVENT respiratory infections that enter the body through the mucosa of the mouth/throat, nose, & eyes.
To PREVENT respiratory infections requires a strong innate immune system with mucosal immunity and secretory IgA to stop the respiratory infection at the mucosal and epithelial barriers (stopping the infection OUTSIDE your body and PREVENTING the infection from getting INSIDE your body).
And this is also where the CTLs are supposed to do their cell-destroying activities. When epithelial cells in the mouth/throat, nose, & eyes are infected (like can happen with respiratory diseases) the Killer T-cells will kill those infected cells.
Epithelial cells at the epithelial barrier can be quickly replaced, usually in just a few days in most people. But injections bypass your body's natural protections and send their payload into your body, where that payload can enter your lymph system and bloodstream.
And in the case of the modified mRNA-LNP gene "therapy" injections, this can be disastrous, starting with the immune system attack response against transfected cells of tissues & organs (INSIDE your body) that are now making foreign non-self proteins.
Replacing cells from now damaged tissues and organs inside your body is a complex process that can take weeks or longer, with some areas unable to be repaired at all.
The modification of natural mRNA with synthetic n1-methyl pseudouridine made the modified mRNA longer lasting and resistant to the body’s natural breakdown processes. A Nobel Prize was awarded specifically for this use of longer lasting pseudouridine in the COVID modified mRNA injections.
The synthetic pseudouridine modified mRNA is causing a +1 ribosomal frameshift, as well as a reverse reading, so some people may make spike proteins AND mystery (or junk) non-self proteins.
Studies have found that an antibody subclass switch to IgG4 can occur between mRNA shot #2 & #3, which is sending a stand-down signal to the immune system, essentially telling the immune system to tolerate and ignore the (toxic pathogenic) spike proteins instead of actively fighting to clear the spike from the body.
And people who are getting "booster" after "booster" are repeatedly triggering these immune system activities and causing persistent systemic inflammation, which can cause hyper-immune and autoimmune responses...and then possible immune system exhaustion as your immune system becomes overwhelmed.
Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.
And then there's the plasmid DNA contamination (with the oncogenic SV-40 promotor sequence) that's been discovered. There are a number of ways in which integration into the human genome is possible...
And more...
I am not a doctor…so PLEASE let me know of any corrections that need to be made if I have misstated something…
But tragically, I think the injuries, disabilities, and deaths from these modified mRNA-LNP gene “therapy” injections prove that the COVID shots have been an IMMUNOLOGICAL CATASTROPHE.
Footnote:
Credit to Dr. Sucharit Bhakdi, Dr. Mike Yeadon, Dr. Kevin Stillwagon, & Dr. Ryan Cole for their videos & articles from which I furthered my understanding of human immunology and the essential component of Self vs. Non-self.
Portions of my 2 comments relied on my notes from their work, as well as other doctors' and scientists' work from my over 10,000 hours researching all things "COVID" and the modified mRNA-LNP gene "therapy" injections since 2020. But as I am not a professional researcher, either, I am sorry to say that I neglected to keep proper citations.
Thats an excellent breakdown, I'd consider adding the Endotoxin contamination and how they labelled it adjuvant to ensure the quantity data was hidden by being a "trade secret"
Any chance you can message me it so I can copy/paste use it to share via text in Australia?
Not trying to steal your work but can see the value and time saved for me.
Unfortunately it's too difficult on a cheap phone with largish hands. Perhaps ask people to direct message you studies etc and if they're freaks ignore them.
Geoff Pain writes about the Endotoxin, others think it's only an immediate issue but I suspect he's onto something and perhaps bigger then the vaxx. Both sides have a point but it was categorised as an adjuvant in a gene therapy that has no virus in it and the technology is completely different from an adjuvant reliant vaccine.
As you know the LNPs are highly inflammatory in themselves as is LPS so why is it really there?
To the nahsayers to Geoffs message eaky gut can produce bowel Endotoxin release but that is not the same as being distributed systemically and intercellularly. Every LNP will have it stuck to the surface and encapsulated within it, potentially projecting it from the bodies removal systems
As one of Mark Crispin Millers “Died Suddenly “ researchers , the phrase “brief illness” is now very common within a multitude of obituaries. My experience, where secondary corroboration is available, usually is code for “turbo cancer”. Anecdotal stories abound about younger and younger people who develop absurd types of cancer. Unfortunately this exhaustive compilation of factual evidence will only be appreciated by the unvaccinated.
Point 8 re Turbo Alzheimers has been noted in many people too and, although generally accepted these days as a normal development of aging, Dr Chris Exley says aluminium found in brains of deceased Alzheimer patients and aluminium being the adjuvant in flu jabs! I personally know someone, now deceased, who's cognative decline only started after jab 2, mild at first, accelerated by jab 3, and by jab 4, unable to watch and follow TV prog, read anything, use his tablet for internet, spending his time longer in bed, or just staring at the wall. I know 8 who suddenly developed cancers since jabs, fortunately no young people, 7 are dead.
Thank you to all the brave doctors & scientists and all the people of the world with curiosity, integrity, and strength of character who have risked so much to get this info out into the world.
The mRNA shots were/are always going to be an immunological catastrophe for humanity.
The mechanism of action (using mRNA instructions to turn one’s own cells into foreign non-self “spike protein factories”) is the primary mechanism of harm.
The primary danger of the COVID-19 mRNA injections has always been one’s own immune system’s attack response by the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells):
The COVID-19 mRNA injections must be recalled from the market and mRNA-based products must be banned because the modified mRNA-LNP genetic technology platform is fundamentally flawed & dangerous by design.
These modified mRNA-LNP COVID-19 injections, that trigger one's own immune system to attack & kill one's own formerly healthy cells (that have been instructed to produce/express foreign, non-self proteins), no matter where those cells are in the body, never should have been made available to the public in the first place.
When the (designed to be long-lasting) n1-methyl pseudouridine modified mRNA transfects one's cells, and gives instructions for the ribosomes to make & express foreign non-self proteins (such as the toxic SARS-CoV-2 spike protein), one's immune system sends the CD8+ cytotoxic T lymphocytes (CTLs) to kill those formerly healthy cells that are now making & expressing non-self proteins.
It is the mission of these CD8+ CTLs to seek out and destroy any such transfected cell that is making foreign non-self proteins. That’s what they do…
Due to the biodistribution properties of the lipid nanoparticles, the encased modified mRNA can go anywhere in the body, including crossing the blood-brain and placental barriers...The LNP "delivery vehicles" traveled to different parts of the body in different people.
Expressing any foreign protein is fatal to the cell doing the expressing. The reason is, our bodies are protected by being able to distinguish ourselves from things that shouldn't be there. Anything non-self will trigger immune destruction of the cells & tissues involved.
Some people will express lots of foreign proteins in vulnerable locations. Others express less in less vulnerable areas.
The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms…
If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signaling (increasing your risk of fast-growing and aggressive cancers)…
And more…
There's no limit to the horrible consequences of injecting into your body something that triggers your own immune system to attack & kill your own formerly healthy cells & tissues.
The public “health” agencies, the COVID “authorities”, & the “mainstream” media fraudulently marketed these experimental mRNA gene “therapy” products as “safe & effective vaccines”. Trusting people thought that they were being presented with the choice (or the mandate) as to whether or not to take a “safe & effective vaccine”…But that was/is a deceptively false “choice”…
The COVID-19 mRNA injections are NOT safe, they are NOT effective, and they are NOT vaccines.
These modified mRNA-LNP gene “therapy” injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the fraudulent mislabeling as “vaccines”. (And because of the EUA & “countermeasure” designations under the Project BioShield Act & PREP Act).
NO ONE should have ever had the “choice” of taking these gene “therapy” injections because the modified mRNA-LNP genetic technology platform is fundamentally flawed & dangerous by design.
The danger is NOT limited to just getting more COVID “boosters”. ANY mRNA gene “therapy” product that transfects your cells and instructs those cells to produce foreign non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues (the role of the Killer T-cells is to monitor ALL the cells of the body, ready to destroy/kill any that express foreign, non-self proteins). This makes EVERY mRNA-based injected product harmful by design.
No one who took these modified mRNA-LNP COVID injections made an informed decision. Most people had no clue about what they allowed to be injected into their bodies...
Also most people still do not understand that the devastating harms inflicted upon people over the last few years was intentional:
https://rumble.com/v6qcb0y-dr.-david-martin-mar-06-2025-edmonton-alberta-replay.html
Part 2
AFTER the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells) attack response to modified mRNA transfected cells of tissues & organs inside your body:
After the primary immune system attack response by the cytotoxic T lymphocytes (CTLs), resulting in varying degrees of tissue damage & pathology in different people, a lot happens...
The CTLs will not be able to kill every cell making non-self (spike) protein, so some amount of foreign (spike) protein will get made & released from your cells. That amount will also vary from person to person.
Specialized cells called antigen-presenting cells, especially dendritic cells and macrophages, spring into action. Long story short…you will get serum antibodies made against those foreign proteins which is the stated goal of any shot called a vaccine.
But that can take up to 2 weeks, and during that time, the foreign non-self (spike) proteins are biologically active and will attach to various cellular receptors, resulting in a whole new level of possible tissue destruction.
Now your immune system will activate macrophages & neutrophils that will kill THOSE cells through inflammatory pathways, regardless of whether or not the non-self proteins are toxic themselves.
And if the non-self proteins ARE toxic, like the pathogenic spike proteins, they can cause problems like tissue damage all by themselves without your immune system even being involved at that point.
But your adaptive immune system has done its job & you've made your serum antibodies by now! Yippee!
Too bad those (non-neutralizing, leaky) serum antibodies can only REACT to a (SARS-CoV-2) infection...it is biologically impossible for serum antibodies (in the blood) to PREVENT respiratory infections that enter the body through the mucosa of the mouth/throat, nose, & eyes.
To PREVENT respiratory infections requires a strong innate immune system with mucosal immunity and secretory IgA to stop the respiratory infection at the mucosal and epithelial barriers (stopping the infection OUTSIDE your body and PREVENTING the infection from getting INSIDE your body).
And this is also where the CTLs are supposed to do their cell-destroying activities. When epithelial cells in the mouth/throat, nose, & eyes are infected (like can happen with respiratory diseases) the Killer T-cells will kill those infected cells.
Epithelial cells at the epithelial barrier can be quickly replaced, usually in just a few days in most people. But injections bypass your body's natural protections and send their payload into your body, where that payload can enter your lymph system and bloodstream.
And in the case of the modified mRNA-LNP gene "therapy" injections, this can be disastrous, starting with the immune system attack response against transfected cells of tissues & organs (INSIDE your body) that are now making foreign non-self proteins.
Replacing cells from now damaged tissues and organs inside your body is a complex process that can take weeks or longer, with some areas unable to be repaired at all.
The modification of natural mRNA with synthetic n1-methyl pseudouridine made the modified mRNA longer lasting and resistant to the body’s natural breakdown processes. A Nobel Prize was awarded specifically for this use of longer lasting pseudouridine in the COVID modified mRNA injections.
The synthetic pseudouridine modified mRNA is causing a +1 ribosomal frameshift, as well as a reverse reading, so some people may make spike proteins AND mystery (or junk) non-self proteins.
Studies have found that an antibody subclass switch to IgG4 can occur between mRNA shot #2 & #3, which is sending a stand-down signal to the immune system, essentially telling the immune system to tolerate and ignore the (toxic pathogenic) spike proteins instead of actively fighting to clear the spike from the body.
And people who are getting "booster" after "booster" are repeatedly triggering these immune system activities and causing persistent systemic inflammation, which can cause hyper-immune and autoimmune responses...and then possible immune system exhaustion as your immune system becomes overwhelmed.
Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.
And then there's the plasmid DNA contamination (with the oncogenic SV-40 promotor sequence) that's been discovered. There are a number of ways in which integration into the human genome is possible...
And more...
I am not a doctor…so PLEASE let me know of any corrections that need to be made if I have misstated something…
But tragically, I think the injuries, disabilities, and deaths from these modified mRNA-LNP gene “therapy” injections prove that the COVID shots have been an IMMUNOLOGICAL CATASTROPHE.
Footnote:
Credit to Dr. Sucharit Bhakdi, Dr. Mike Yeadon, Dr. Kevin Stillwagon, & Dr. Ryan Cole for their videos & articles from which I furthered my understanding of human immunology and the essential component of Self vs. Non-self.
Portions of my 2 comments relied on my notes from their work, as well as other doctors' and scientists' work from my over 10,000 hours researching all things "COVID" and the modified mRNA-LNP gene "therapy" injections since 2020. But as I am not a professional researcher, either, I am sorry to say that I neglected to keep proper citations.
Thank you Kelly for your highly informative and exceptional comment.
Sonia, THANK YOU for your tireless efforts to uncover & expose the truth about these mRNA shots.
Hi Kelly
Thats an excellent breakdown, I'd consider adding the Endotoxin contamination and how they labelled it adjuvant to ensure the quantity data was hidden by being a "trade secret"
Any chance you can message me it so I can copy/paste use it to share via text in Australia?
Not trying to steal your work but can see the value and time saved for me.
Thank you, Damon!
I am not concerned with credit or recognition, so please feel free to copy/paste & share anywhere and with anyone.
Can you copy/paste straight from Substack comments?
I may have to add another footnote to the 2-part comment encouraging people who feel so inclined to copy/paste and share!
:)
Unfortunately it's too difficult on a cheap phone with largish hands. Perhaps ask people to direct message you studies etc and if they're freaks ignore them.
Geoff Pain writes about the Endotoxin, others think it's only an immediate issue but I suspect he's onto something and perhaps bigger then the vaxx. Both sides have a point but it was categorised as an adjuvant in a gene therapy that has no virus in it and the technology is completely different from an adjuvant reliant vaccine.
As you know the LNPs are highly inflammatory in themselves as is LPS so why is it really there?
To the nahsayers to Geoffs message eaky gut can produce bowel Endotoxin release but that is not the same as being distributed systemically and intercellularly. Every LNP will have it stuck to the surface and encapsulated within it, potentially projecting it from the bodies removal systems
i.e. Endotoxin binding protein.
As one of Mark Crispin Millers “Died Suddenly “ researchers , the phrase “brief illness” is now very common within a multitude of obituaries. My experience, where secondary corroboration is available, usually is code for “turbo cancer”. Anecdotal stories abound about younger and younger people who develop absurd types of cancer. Unfortunately this exhaustive compilation of factual evidence will only be appreciated by the unvaccinated.
Only 17 induced cancer potentialities? Good God it’s far worse than cancer, than death!
What could possibly be worse than cancer or death? Total Govt. control over every aspect of our lives!
I declare “Die-Free,” of live in “Tyranny!” The choice doesn’t seem to matter to us anymore, now does it?
Our Govt. has made the choice for us! God Help Us All!
AJR
Point 8 re Turbo Alzheimers has been noted in many people too and, although generally accepted these days as a normal development of aging, Dr Chris Exley says aluminium found in brains of deceased Alzheimer patients and aluminium being the adjuvant in flu jabs! I personally know someone, now deceased, who's cognative decline only started after jab 2, mild at first, accelerated by jab 3, and by jab 4, unable to watch and follow TV prog, read anything, use his tablet for internet, spending his time longer in bed, or just staring at the wall. I know 8 who suddenly developed cancers since jabs, fortunately no young people, 7 are dead.